JPH0613073A - Cadmium negative electrode for alkaline storage battery - Google Patents

Cadmium negative electrode for alkaline storage battery

Info

Publication number
JPH0613073A
JPH0613073A JP4205854A JP20585492A JPH0613073A JP H0613073 A JPH0613073 A JP H0613073A JP 4205854 A JP4205854 A JP 4205854A JP 20585492 A JP20585492 A JP 20585492A JP H0613073 A JPH0613073 A JP H0613073A
Authority
JP
Japan
Prior art keywords
electrode
cadmium
negative electrode
reinforcing material
paste
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP4205854A
Other languages
Japanese (ja)
Other versions
JP3241441B2 (en
Inventor
Seiji Ishizuka
清司 石塚
Kazuo Furushima
和夫 古嶋
Hiroshi Suzuki
博士 鈴木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
FDK Twicell Co Ltd
Original Assignee
Toshiba Battery Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toshiba Battery Co Ltd filed Critical Toshiba Battery Co Ltd
Priority to JP20585492A priority Critical patent/JP3241441B2/en
Publication of JPH0613073A publication Critical patent/JPH0613073A/en
Application granted granted Critical
Publication of JP3241441B2 publication Critical patent/JP3241441B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Landscapes

  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To extend the surface area of an electrode to increase O2 gas reacting part and improve O2 gas consuming performance by adding a reinforcing material not to the surface layer of the electrode but only to the electrode inner layer. CONSTITUTION:Cadmium oxide, Ni powder, a reinforcing material fiber, and ethylene glycol solution of carboxymethyl cellulose are kneaded together to prepare an active material paste. This is applied to a Ni-plated punched base for collector followed by heating and drying to form a cadmium oxide electrode. On the other hand, metal cadmium, carboxymethyl cellulose, fluorine resin dispersion, and ion exchange water are kneaded together to prepare a metal cadmium paste. This is applied to both surface of the cadmium oxide electrode followed by heating and drying to form a cadmium negative electrode. According to this negative electrode, since O2 gas generated at overcharge of battery can be quickly absorbed, an alkaline storage battery conforming to quick charge can be provided.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はアルカリ蓄電池に用いる
カドミウム負極の改良に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an improved cadmium negative electrode used in alkaline storage batteries.

【0002】[0002]

【従来の技術】近年アルカリ蓄電池において、ペースト
式カドミウム負極は、焼結式カドミウム負極と比べて、
製造工程が簡単でありコストが安く、また高いエネルギ
ー密度が得られるなどの長所を持つため、より多く用い
られるようになってきた。しかし、焼結式カドミウム負
極に比べて電極の導電性が劣るため、過充電時に正極よ
り発生する酸素ガスの吸収性能が悪く、密閉型電池に使
用すると電池の内圧が上昇し易いという欠点があった。
そのため、電池に組み込む前にカドミウム負極を化成
し、放電予備量としての金属カドミウムを形成し、導電
性を付与する方法が採られているが、この方法はペース
ト式カドミウム負極の製造工程の簡単さやコスト上の長
所が損なわれてしまった。
2. Description of the Related Art In recent years, in alkaline storage batteries, the paste type cadmium negative electrode has a
Since it has advantages such as a simple manufacturing process, low cost, and high energy density, it has been used more and more. However, the conductivity of the electrode is inferior to that of the sintered cadmium negative electrode, so that the oxygen gas generated from the positive electrode during overcharging is poorly absorbed, and when used in a sealed battery, the internal pressure of the battery tends to rise. It was
Therefore, a method of forming a cadmium negative electrode before incorporating it into a battery, forming metal cadmium as a discharge reserve amount, and imparting conductivity is adopted, but this method is simple in the manufacturing process of the paste type cadmium negative electrode. The cost advantage has been compromised.

【0003】[0003]

【発明が解決しようとする課題】このような問題点を解
決するために特開昭54−50843号公報において、
ペースト状活物質層の表面に金属カドミウムの層を形成
することで、酸素ガス吸収性能が優れ化成工程を省略で
きるとされているが、このような方法だけでは製造工程
上必要な電極の物理的強度や酸素ガス吸収性能におい
て、まだ不十分なものであった。一方ペースト式カドミ
ウム負極をフッ素樹脂の分散液に含浸し、電極活物質に
撥水性を持たせ、酸素ガスと電解液との反応面積を増や
し、酸素ガス吸収性能や電極の物理強度を向上できるこ
とが提案されているが、それでも焼結式カドミウム負極
と同等の酸素ガス吸収性能や電極の物理的強度を得るに
は至っていない。
SUMMARY OF THE INVENTION In order to solve such a problem, Japanese Patent Laid-Open No. 54-50843 discloses that
It is said that by forming a layer of metal cadmium on the surface of the paste-like active material layer, the oxygen gas absorption performance is excellent and the chemical conversion step can be omitted. It was still insufficient in strength and oxygen gas absorption performance. On the other hand, it is possible to impregnate a paste-type cadmium negative electrode with a dispersion liquid of a fluororesin, to make the electrode active material water-repellent, to increase the reaction area between oxygen gas and the electrolytic solution, and to improve the oxygen gas absorption performance and the physical strength of the electrode. Although proposed, the oxygen gas absorption performance and the physical strength of the electrode equivalent to those of the sintered cadmium negative electrode have not yet been obtained.

【0004】本発明はこのような従来の欠点を解消し、
比較的廉価で、ペースト式カドミウム負極の製造工程に
おいて、化成をすることなしに酸素ガス吸収性能や電極
の物理的強度が優れたアルカリ蓄電池用カドミウム負極
を得ることを目的とする。
The present invention overcomes these drawbacks of the prior art,
An object of the present invention is to obtain a cadmium negative electrode for alkaline storage batteries, which is relatively inexpensive and has excellent oxygen gas absorption performance and excellent physical strength of the electrode without chemical conversion in the manufacturing process of the paste type cadmium negative electrode.

【0005】[0005]

【課題を解決するための手段】本発明は、酸化カドミウ
ムを主体とした内部層と、金属カドミウムを主体とした
表面層とを有するカドミウム負極において、該内部層が
補強材を有し、表面層は補強材を有していないことを特
徴とするアルカリ蓄電池用カドミウム負極である。
The present invention relates to a cadmium negative electrode having an inner layer mainly composed of cadmium oxide and a surface layer mainly composed of metal cadmium, the inner layer having a reinforcing material, and the surface layer Is a cadmium negative electrode for an alkaline storage battery, which has no reinforcing material.

【0006】[0006]

【作用】一般にニッケルカドミウム電池の密閉化は、過
充電時に正極から発生する酸素ガスを負極上で消費する
ことにより得ている。この反応は負極表面と電解液と酸
素ガスが接触して始めて起こる。一方電極の強度を保持
するために電極中に補強材を添加するが、本発明は補強
材を電極内部層にのみ添加し、電極の表面層は補強材を
添加しないため、表面層の表面積をより広くでき、酸素
ガス反応に寄与する反応部位が増えるため、結局酸素ガ
スの消費能力が向上するようになる。
In general, the sealed nickel-cadmium battery is obtained by consuming oxygen gas generated from the positive electrode on the negative electrode during overcharge. This reaction occurs only when the surface of the negative electrode, the electrolytic solution and oxygen gas come into contact with each other. On the other hand, in order to maintain the strength of the electrode, a reinforcing material is added to the electrode, but in the present invention, the reinforcing material is added only to the electrode inner layer, and the surface layer of the electrode does not contain the reinforcing material. Since it can be made wider and the number of reaction sites that contribute to the oxygen gas reaction increases, the consumption capacity of oxygen gas will eventually improve.

【0007】[0007]

【実施例】以下、実施例により本発明を詳細に説明す
る。酸化カドミウム95重量部とニッケル粉末5重量部
と補強材として繊維と、カルボキシルメチルセルロース
のエチレングリコール溶液と、ポリビニルアルコールの
エチレングリコール溶液とを、混練して得た活物質ペー
ストを、集電体であるニッケルメッキを施したパンチド
基板に塗工し、約120℃で2時間乾燥して酸化カドミ
ウム電極を得た。次に、金属カドミウム100重量部と
カルボキシルメチルセルロースとフッ素樹脂ディスパー
ジョンとイオン交換水との混合物を混練して、金属カド
ミウムペーストを得た。このペーストを前記酸化カドミ
ウム電極の両面に塗工し、約150℃で乾燥することに
より、本発明によるカドミウム負極aを得た。この本発
明による電極aの比較例として、金属カドミウムペース
トに補強材として繊維を添加した表面層を有するカドミ
ウム負極bを作製した。
The present invention will be described in detail below with reference to examples. An active material paste obtained by kneading 95 parts by weight of cadmium oxide, 5 parts by weight of nickel powder, fibers as a reinforcing material, an ethylene glycol solution of carboxymethyl cellulose, and an ethylene glycol solution of polyvinyl alcohol is a current collector. It was applied on a nickel-plated punched substrate and dried at about 120 ° C. for 2 hours to obtain a cadmium oxide electrode. Then, a mixture of 100 parts by weight of metal cadmium, carboxymethyl cellulose, fluororesin dispersion and ion-exchanged water was kneaded to obtain a metal cadmium paste. This paste was applied to both surfaces of the cadmium oxide electrode and dried at about 150 ° C. to obtain a cadmium negative electrode a according to the present invention. As a comparative example of the electrode a according to the present invention, a cadmium negative electrode b having a surface layer obtained by adding fibers as a reinforcing material to a metal cadmium paste was prepared.

【0008】これらの負極を公知のペーストニッケル正
極を用いてそれぞれ電池A、Bを構成した。これらの電
池を公称容量に対して、1Cで300%の過充電を行な
ったときの電池内を、図1に示した。電池Bと比較して
電池Aの方が低い内圧を示した。これは電池Aのカドミ
ウム負極は、電極表面層に補強材が添加されてない分、
表面層の多孔度が大きく、酸素ガスを消費する反応部位
が広いためと考えられる。
Batteries A and B were constructed by using these negative electrodes as known nickel paste positive electrodes. FIG. 1 shows the inside of the batteries when these batteries were overcharged at 1 C to 300% of the nominal capacity. Battery A showed a lower internal pressure than battery B. This is because the cadmium negative electrode of Battery A has no reinforcing material added to the electrode surface layer,
It is considered that the surface layer has a large porosity and the reaction site that consumes oxygen gas is wide.

【0009】[0009]

【発明の効果】このように本発明によれば、電池の過充
電時に発生する酸素ガスを、速やかに吸収できるため、
急速充電に対応した工業的価値の高いアルカリ蓄電池を
得ることができる。
As described above, according to the present invention, the oxygen gas generated when the battery is overcharged can be quickly absorbed.
It is possible to obtain an alkaline storage battery with high industrial value that is compatible with quick charging.

【図面の簡単な説明】[Brief description of drawings]

【図1】過充電に対する電池の内圧の変化を示した比較
図である。
FIG. 1 is a comparative diagram showing changes in internal pressure of a battery due to overcharge.

【符号の説明】[Explanation of symbols]

A…本発明電池 B…比較例電池 A: battery of the present invention B: comparative battery

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 酸化カドミウムを主体とした内部層と、
金属カドミウムを主体とした表面層とを有するカドミウ
ム負極において、該内部層が補強材を有し、表面層が補
強材を有していないことを特徴とするアルカリ蓄電池用
カドミウム負極。
1. An inner layer mainly composed of cadmium oxide,
A cadmium negative electrode having a surface layer containing metal cadmium as a main component, wherein the inner layer has a reinforcing material and the surface layer does not have a reinforcing material.
JP20585492A 1992-06-24 1992-06-24 Cadmium negative electrode for alkaline storage batteries Expired - Fee Related JP3241441B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20585492A JP3241441B2 (en) 1992-06-24 1992-06-24 Cadmium negative electrode for alkaline storage batteries

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20585492A JP3241441B2 (en) 1992-06-24 1992-06-24 Cadmium negative electrode for alkaline storage batteries

Publications (2)

Publication Number Publication Date
JPH0613073A true JPH0613073A (en) 1994-01-21
JP3241441B2 JP3241441B2 (en) 2001-12-25

Family

ID=16513814

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20585492A Expired - Fee Related JP3241441B2 (en) 1992-06-24 1992-06-24 Cadmium negative electrode for alkaline storage batteries

Country Status (1)

Country Link
JP (1) JP3241441B2 (en)

Also Published As

Publication number Publication date
JP3241441B2 (en) 2001-12-25

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